Santagati S, Melcangi R C, Celotti F, Martini L, Maggi A
Milano Molecular Pharmacology Laboratory, Institute of Pharmacological Sciences, Italy.
J Neurochem. 1994 Dec;63(6):2058-64. doi: 10.1046/j.1471-4159.1994.63062058.x.
Estrogens derived from the aromatization of androgens are believed to be responsible for the induction of the sexual differentiation of the CNS interacting with specific estrogen receptors (ER) present in developing neurons. However, the brain cellular distribution of ER is not so well documented. The aim of this study was to investigate the qualitative and quantitative expression of ER mRNA in well characterized cultures of rat type 1 and type 2 astrocytes and of oligodendrocytes by polymerase chain reaction. A series of amplifications with a set of primers spanning along the entire ER mRNA was utilized in the different types of glial cells, in a positive control (uterus), and in a negative control (SK-N-BE cell line) previously shown to be devoid of ER. The data obtained show that ER mRNA is expressed in all three types of glial cell analyzed in almost equal amounts, which are 25-50 times lower than those in the uterus. The mRNA expressed in the glia is homologous with that expressed in the uterine tissue.
雄激素芳香化产生的雌激素被认为与发育中的神经元中存在的特定雌激素受体(ER)相互作用,从而诱导中枢神经系统的性别分化。然而,ER在脑内的细胞分布尚无充分记载。本研究旨在通过聚合酶链反应,研究ER mRNA在特征明确的大鼠1型和2型星形胶质细胞以及少突胶质细胞培养物中的定性和定量表达。在不同类型的神经胶质细胞、阳性对照(子宫)和先前已证明不含ER的阴性对照(SK-N-BE细胞系)中,使用一组沿整个ER mRNA跨度的引物进行了一系列扩增。获得的数据表明,ER mRNA在所有三种分析的神经胶质细胞类型中均有表达,表达量几乎相等,比子宫中的表达量低25-50倍。神经胶质细胞中表达的mRNA与子宫组织中表达的mRNA同源。